BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWERED PATIENT ROTATION BED

    MDR report key: 3080050 · Received April 26, 2013

    Report

    Report Number
    1031452-2013-00798
    Event Type
    Malfunction
    Date Received
    April 26, 2013
    Report Date
    April 2, 2013
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    IKZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    POTENTIAL FOR INJURY ASSOCIATED WITH A FOOT MOTOR ON A 5310IVC SEMI-ELECTRIC BED DRIFTING DOWN AFTER BEING RAISED. THIS CREATES THE POTENTIAL FOR A FOOT END BED DROP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    182807 POWERED PATIENT ROTATION BED 890.5225 IKZ INVACARE FLORIDA OPERATIONS 5301IVC

    Patients

    Seq Age Sex Outcome Treatment
    1 Other